GB2382455A - Fuel cell fluid flow field plates - Google Patents
Fuel cell fluid flow field plates Download PDFInfo
- Publication number
- GB2382455A GB2382455A GB0126688A GB0126688A GB2382455A GB 2382455 A GB2382455 A GB 2382455A GB 0126688 A GB0126688 A GB 0126688A GB 0126688 A GB0126688 A GB 0126688A GB 2382455 A GB2382455 A GB 2382455A
- Authority
- GB
- United Kingdom
- Prior art keywords
- fluid flow
- channel
- field plate
- flow field
- bipolar
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M8/00—Fuel cells; Manufacture thereof
- H01M8/02—Details
- H01M8/0202—Collectors; Separators, e.g. bipolar separators; Interconnectors
- H01M8/0258—Collectors; Separators, e.g. bipolar separators; Interconnectors characterised by the configuration of channels, e.g. by the flow field of the reactant or coolant
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M8/00—Fuel cells; Manufacture thereof
- H01M8/02—Details
- H01M8/0202—Collectors; Separators, e.g. bipolar separators; Interconnectors
- H01M8/0258—Collectors; Separators, e.g. bipolar separators; Interconnectors characterised by the configuration of channels, e.g. by the flow field of the reactant or coolant
- H01M8/026—Collectors; Separators, e.g. bipolar separators; Interconnectors characterised by the configuration of channels, e.g. by the flow field of the reactant or coolant characterised by grooves, e.g. their pitch or depth
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M8/00—Fuel cells; Manufacture thereof
- H01M8/02—Details
- H01M8/0202—Collectors; Separators, e.g. bipolar separators; Interconnectors
- H01M8/0258—Collectors; Separators, e.g. bipolar separators; Interconnectors characterised by the configuration of channels, e.g. by the flow field of the reactant or coolant
- H01M8/0263—Collectors; Separators, e.g. bipolar separators; Interconnectors characterised by the configuration of channels, e.g. by the flow field of the reactant or coolant having meandering or serpentine paths
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M8/00—Fuel cells; Manufacture thereof
- H01M8/02—Details
- H01M8/0202—Collectors; Separators, e.g. bipolar separators; Interconnectors
- H01M8/0258—Collectors; Separators, e.g. bipolar separators; Interconnectors characterised by the configuration of channels, e.g. by the flow field of the reactant or coolant
- H01M8/0265—Collectors; Separators, e.g. bipolar separators; Interconnectors characterised by the configuration of channels, e.g. by the flow field of the reactant or coolant the reactant or coolant channels having varying cross sections
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M8/00—Fuel cells; Manufacture thereof
- H01M8/24—Grouping of fuel cells, e.g. stacking of fuel cells
- H01M8/2465—Details of groupings of fuel cells
- H01M8/2483—Details of groupings of fuel cells characterised by internal manifolds
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/30—Hydrogen technology
- Y02E60/50—Fuel cells
Abstract
A bipolar fluid flow field plate for a fuel cell delivers fuel to a porous anode electrode and oxidant to an adjacent porous cathode electrode. The flow field plate comprises an electrically conductive, non-porous sheet into which fluid flow conduits 36, 37 are formed. A first fluid flow channel is patterned into a first face of the sheet and a second fluid flow channel patterned into the opposite face of the sheet. The pattern of the first channel comprises an interdigitated comb that co-operates with a pattern of the second channel comprising a continuous serpentine path, so that no portion of the first channel directly overlies the pattern of the second channel over a substantial active area of the sheet. This allows the channels to be formed with combined depths that exceed the total plate thickness, thereby increasing fluid flow volumes.
Description
FUEL CELL FLUID FLOW FIELD PLATES
The present invention relates to fuel cells, and in particular to flow field
plates suitable for use in solid polymer electrolyte fuel cells, which flow 5 field plates act as fluid delivery conduits to electrode surfaces of the fuel
cell. Conventional electrochemical fuel cells convert fuel and oxidant into electrical energy and a reaction product. A typical layout of a conventional 10 fuel cell 10 is shown in figure 1 which, for clarity, illustrates the various layers in exploded form. A solid polymer ion transfer membrane 11 is sandwiched between an anode 12 and a cathode 13. The polymer membrane allows protons to traverse the membrane, but blocks the passage of electrons. Typically, the anode 12 and the cathode 13 are both formed from 15 an electrically conductive, porous material such as porous carbon, to which small particles of platinum andlor other precious metal catalyst are bonded.
The anode 12 and cathode 13 are often bonded directly to the respective adjacent surfaces of the membrane 11. This combination is commonly referred to as the membrane-electrode assembly, or MEA.
Sandwiching the polymer membrane and porous electrode layers is an anode fluid flow field plate 14 and a cathode fluid flow field plate 15. Intermediate
backing layers 12a and 13a may also be employed between the anode fluid flow field plate 14 and the anode 12 and similarly between the cathode fluid
25 flow field plate 15 and the cathode 13. The backing layers are of a porous
nature and fabricated so as to ensure effective diffusion of gas to and from the anode and cathode surfaces as well as assisting in the management of water vapour and liquid water. Throughout the present specification,
references to the electrodes (anode and/or cathode) are intended to include 30 electrodes with or without such a backing layer.
The fluid flow field plates 14, IS are formed from an electrically conductive,
non-porous material by which electrical contact can be made to the respective anode electrode 12 or cathode electrode 13. At the same time, the 5 fluid flow field plates must enable the delivery and/or exhaust of fluid fuel,
oxidant and/or reaction product (and/or other diluent gases not taking part in the reaction) to or from the porous electrodes. This is conventionally effected by forming fluid flow passages in a surface of the fluid flow field
plates, such as grooves or channels 16 in the surface presented to the porous 1 0 electrodes.
With reference also to figure 2, it will be seen that one prior art
configuration of fluid flow channel, such as that taught in US 5,108,849 is a serpentine structure 20 in a face of the anode 14 (or cathode) having an inlet 15 manifold 21 and an outlet manifold 22.
In a typical application, in the anode fluid flow field plate 14, hydrogen gas
is delivered into the serpentine channel 20 from the inlet manifold 21. In the cathode fluid flow field plate 15, oxidant (ea. oxygen gas) is delivered into
20 the serpentine channel 20 from the inlet manifold. Because it is important to maintain a good supply of oxygen to the porous cathode electrode 13, and because reaction product (water) accumulates therein, it is often important to maintain a high flow rate of oxidant gas through the serpentine channel 20 from the inlet manifold 21 to the outlet manifold 22, to expel depleted gas 25 supply and product water.
Because the voltage produced by a single fuel cell is quite low (typically approximately 0.7 V), conventionally multiple cells are connected in series with the electrically conductive, cathode fluid flow field plate of one cell
being placed in electrical contact with the adjacent anode fluid flow field
plate of the next cell.
As shown in figure 3, in order to simplify construction of a seriesconnected 5 array or "stack" 30 of fuel cells, it has been proposed in the prior art to
utilise a single fluid flow field plate 31, 32 shared between adjacent cells.
By way of example, cell 34 shares plate 32 with adjacent cell 35. The left hand face (as represented in figure 3) of bipolar plate 32 acts as a cathode for cell 34 and incorporates cathode fluid flow channels 36, while the right hand 10 face acts as an anode for cell 35 and incorporates anode fluid flow channels 37. Thus, in bipolar fluid flow field plate 32, channels are formed in both
faces of the plate and the number of separate fluid flow field plates required
in the stack of fuel cells is consequently reduced.
15 The present invention is directed to providing still further improvements in the construction of fluid flow field plates and a reduction in the dimensions
of a fuel cell stack.
According to one aspect, the present invention provides a bipolar fluid flow 20 field plate for a fuel cell comprising an electrically conductive, non-porous
sheet having a first fluid flow channel patterned into a first face of the sheet and a second fluid flow channel patterned into the opposite face of the sheet, in which the pattern of the first channel is configured to have no portion thereof directly overlying the pattern of the second channel over a 25 substantial area of the sheet.
According to another aspect, the present invention provides a bipolar fluid flow field plate for a fuel cell comprising an electrically conductive, non-
porous sheet having a first fluid flow channel patterned into a first face of 30 the sheet and a second fluid flow channel patterned into the opposite face of
the sheet, in which the combined depth of the first and second channels in an active area of the plate exceeds the total thickness of the plate.
Embodiments of the present invention will now be described by way of 5 example and with reference to the accompanying drawings in which: Figure 1 is an exploded cross-sectional view of a prior art fuel cell;
Figure 2 is a plan view of a prior art fluid flow field plate in the fuel
cell of figure 1; Figure 3 is an exploded cross-sectional view of a prior art series
10 connected fuel cell stack; Figure 4 is a cross-sectional view of a portion of the bipolar fluid flow field plate in figure 3;
Figure 5 is a cross-sectional view of a portion of a bipolar fluid flow field plate according to one aspect of the present invention;
15 Figure 6 is a cross-sectional view of a portion of a bipolar fluid flow field plate according to another aspect of the present invention;
Figure 7 is a schematic plan view of continuous serpentine and interdigitated comb channels formed in opposing faces of the plate of figure 5 or figure 6; 20 Figure 8 is a cross-sectional view of a portion of a bipolar fluid flow field plate showing reduced channel depth crossover portions;
Figure 9 is a cross-sectional view of a portion of a bipolar fluid flow field plate and adjacent porous electrodes with bypass channels therein; and
Figures 1 Oa and 1 Ob are schematic plan views of interrupted 25 serpentine and comb channel patterns to be formed in opposing faces of the plate of figure 5 or figure 6.
A critical factor in the commercial viability of fuel cells is the deliverable energy per unit volume of fuel cell. There is an everincreasing demand to 30 deliver more power per unit volume, and this has led to some improvements
such as the bipolar fluid flow field plate configuration indicated in figure 3
and figure 4. To decrease the dimension of the fuel cell stack still further, the present inventors have recognised that the bipolar plate can be substantially reduced in thickness by co-ordinating channel structures on 5 opposing faces of the plates 31, 32.
In the prior art configuration of figure 4, the thickness of bipolar plates 31,
32 has been determined according to the depth of channel required on both sides of the plate, plus sufficient thickness of plate lying between the 10 channel bottoms to ensure structural integrity of the plate. This is illustrated in figure 4. As shown, the bipolar plate 31, 32 thickness Tp generally equals the anode channel depth, dA plus cathode channel depth, dc plus an intermediate plate thickness, Tj.
15 According to the present invention, the anode and cathode fluid flow channel configurations on both faces of the bipolar plates are coordinated so that the number of cross-over points where the anode channels 37 overlie the cathode channels 36 is reduced, preferably to zero.
20 Where this is effected, the anode and cathode fluid flow channels 36, 37 are themselves co-ordinated in an interleaved fashion as depicted in figure 5. In this configuration, it will be noted that the plate thickness Tp now generally equals the anode channel depth, dA plus cathode channel depth, tic minus a channel depth overlap, To. The channel spacing or wall thickness (SA, SC) 25 on each side of the plate is increased sufficiently to accommodate the width of the intervening channel on the other side of the plate, plus an internal channel spacing Sj within the plate between each adjacent channel on alternating sides of the plate.
s
In figure 5, a rectangular channel profile is shown, as can be conveniently formed using various chemical etching techniques, electrochemical machining, abrasive machining or other suitable material removal processes.
As evident from figure 6, other channel profiles such as a triangular profile 5 can be used to similar effect. In figure 6, however, it will be noted that the particular channel profile allows that the channel spacing SA and Sc on each side of the plate need not be increased to the same extent as in figure 5 in order to maintain an effective internal channel spacing Sj. In these examples, a "past-centre" material removal process is used to form the 10 channels 36, 37 to a depth greater than the centre of the plate thickness.
To allow the use of a "past-centre" material removal process, the configuration of the anode and cathode fluid flow channels are coordinated to avoid any superposition of the channels over a substantial portion, and 15 preferably all, of the active area of the bipolar plate faces.
An exemplary serpentine and interdigitated comb pattern is shown schematically in figure 7. In figure 7, bipolar fluid flow field plate 70
includes a first inlet manifold 71 which preferably comprises an aperture 20 through the full thickness of the plate 70. The first inlet manifold 71 communicates with comb structure channels 74 which are formed on a first surface of the bipolar plate. Comb structure channels 73 direct the fluid to the corresponding first outlet manifold 72, which also preferably comprises an aperture through the full thickness of the plate 70.
A second inlet manifold 75 and a second outlet manifold 76 preferably comprise respective apertures through the full thickness of the plate. On the opposite surface of the bipolar plate, and therefore shown in dashed line form, is a serpentine channel 77 that communicates with the second inlet 30 manifold 75 and the second outlet manifold 76 respectively. In use, gas is
supplied through the second inlet manifold 75, and passed through the serpentine channel 77 from which it is transported into an adjacent porous electrode (via a backing layer if one is used). Unused gas, together with water reaction product is passed out from the serpentine channel 77 into 5 cathode outlet manifold 76.
It will be understood that the view of the channels 73, 74, 77 in figure 7 is schematically represented only, and that the number of "teeth" in each interdigitated comb structure of the channel pattern, as well as the number of 10 turns in the serpentine structure, is considerable. In a typical example, the plate channel density provides 5 channels per centimetre of plate surface. A typical plate having electrode dimensions 10 cm by 10 cm provides a serpentine channel having 25 passes across the width of the plate in one direction, and a pair of interdigitated combs together providing a 15 corresponding number of "teeth" extending across the width of the plate between the serpentine passes.
In a presently preferred configuration having approximately rectangular cross-section channels, a typical bipolar fluid flow field plate thickness Tp is
20 0.8 mm while the anode and cathode channels 73, 74 and 77 have a depth (dA, dc) of approximately 0.5 mm. The channel depth overlap, To is therefore 0.2 mm. Preferably, the channel widths are 0.7 mm, the channel spacings Sc and SA on each side of the bipolar plate are 1.1 mm, and the internal channel spacing Sj is 0.2 mm.
In preferred embodiments, the plate thickness Tp lies in the range 0.3 mm to 1.5 mm, the channel depths dA and dc lie in the range 0.2 mm to 1.1 mm, the channel depth overlap lies in the range 0.1 mm to 0.4 mm, the channel spacings Sc and SA lie in the range 0.5 mm to 1.5 mm and the internal 30 channel spacing lies in the range 0.05 mm to 0.35 mm.
In the preferred configurations shown, both the anode channel 73 and the cathode channel 77 are formed to equal depths, both being greater than half the thickness of the plate. However, it will be understood that the channel 5 depths could be unequal, the material removal process on one side of the bipolar plate being deeper than on the other side.
It will also be understood that the relative widths of the anode and cathode channels can be varied. The varying of relative widths and depths of the 10 anode channels and the cathode channels enables variation in the relative volume of anode channels versus cathode channels, which can be useful for example, in maintaining appropriate fluid flows with different fluids.
A significant number of alternative channel patterns in the bipolar fluid flow IS field plate can be used. Figure 10 shows two alternative such patterns. In
figure 1 Oa, channel pattern 100 comprises a first (ea. anode) channel pattern comprising four comb structures 101, the "teeth" of which communicate with a respective intermediate channel portion 102 by way of forced diffusion through the adjacent porous electrode. It is therefore possible to 20 maintain a fluid flow from manifolds 103 to manifolds 104 via the channels 101 and 102.
Traversing the active area of the bipolar fluid flow field plate (but on the
opposite face thereof) is a second (ea. cathode) channel pattern comprising a 25 pair of continuous, divergent and reconvergent channels 105, 106 which enable a fluid flow to be maintained between manifolds 107 and 108.
It will be understood that the above references to anode and cathode can be reversed, so that the comb patterns are used for cathode channels and the 30 serpentine patterns are used for anode channels.
Figure lOb shows an alternative channel pattern 110 to that of figure lea, in which the continuous split divergent and reconvergent channels 105 are patterned so as to require differing lengths of intermediate channel portions 5 102 in the comb pattern channels 101.
In general terms, the above described embodiments allow for a combination of a continuous divergent and re-convergent fluid flow channel on one side of a bipolar fluid flow field plate together with an interdigitated "comb"
10 style flow channel on the other side of the bipolar fluid flow field plate, both
channels being to a depth that exceeds half the plate thickness. This configuration allows for a large cross-sectional flow area, within each single fluid flow track, for any given plate thickness. This provides an improved volumetric throughput, for any specified pressure drop, within such a track, 15 for a given plate thickness.
It will be observed from figure 7, figure lOa and figure lOb that there are no cross-over points where any part of the anode channel structure superposes any part of the cathode channel structure. This arrangement represents an 20 effective balance between maximising the area of channel on each side of the bipolar fluid flow plate and minimising the plate thickness. Many other geometric patterns of anode and cathode channels may be used which meet this criterion to varying degrees. In the figure lea, lOb embodiments, fluid flow across "discontinuities" in the channels (ea. between channel sections 25 102, 103 is effected by forced diffusion through the adjacent porous electrode (ie. out of the plane of the fluid flow field plate).
With reference to figure 8, it will be recognised that cross-over points could be conveniently arranged, for example, outside the active area of the plate, 30 ea. in the channels leading to each individual tooth of the comb structure. In
the illustration, this is done by intermittently reducing the depth dA of the channel 73 in the region 80 where the channel overlies a transverse channel 77. In this arrangement, it may be desirable to locally increase the width of the channel 73 in region 80 to compensate for the temporary loss of channel 5 depth, thereby maintaining the fluid flow capacity of the channel.
Other methods exist for allowing limited cross-over points where anode fluid flow channels must overlie (ie. traverse) cathode fluid flow channels and where forced diffusion through the adjacent electrode is not completely 1 0 satisfactory.
It has been recognised that the porous electrodes adjacent to the fluid flow field plate and the channels therein can be conveniently fabricated with a
machined, abraded or embossed surface in which small regions of localised 15 channel formed therein can be used to provide a fluid flow path across a discontinuous fluid flow channel in the bipolar plate.
Referring to figure 9, bipolar fluid flow plate 91 includes an anode channel 94 (extending across the drawing, as shown) with a discontinuity in region 20 95 where a cathode channel 96 extends transversely underneath. To provide continuity to the fluid flow indicated by the arrows, a small bypass channel 97 is formed in the surface of the anode 92 which registers with the ends of discontinuous channel 94 in the bipolar fluid flow field plate 91. Bypass
channel 97 thereby allows fluid communication between the ends of the 25 channel 94 on either side of the transverse channel 96' out of the plane of the bipolar plate 91.
Similar structures may be used when a cathode channel needs to traverse an underlying anode channel. Thus, a bypass channel 97 can equally be formed 30 in the surface of a cathode as in the surface of the anode.
Preferably, the bypass channels 97 formed in a porous anode 92 or cathode 93 are of sufficient length only to traverse the region 95 that overlies the transverse channel 96. In a preferred embodiment, the lengths of bypass 5 channels lies in the range 0.1 mm to 2.0 mm. The width and depth of the bypass channels preferably corresponds to the widths and depths of the channels in the bipolar fluid flow field plate with which they communicate.
Preferably, the bypass channels are conned in the porous carbon electrodes using known abrasive removal techniques such as by particle impingement.
With the co-operating anode and cathode fluid flow channels 36, 37 as described above, it will be noted that if identical bipolar plates 32 were to be used in a stack (as depicted in figure 3), this would result in opposing anode and cathode fluid flow channels on either side of the membrane-electrode 15 assembly 11-13 being offset from one another. If it is desired to have them overlying one another, the fluid flow channels of adjacent bipolar plates (ie.
on an alternating basis down a stack) can be laterally offset from one another in order to align anode and cathode flow channels.
20 Although the examples of the present invention have been described in the context of fuel cell devices requiring opposing gas streams, it will be understood that the methodology can be extended to synthesis cells using membrane or diaphragm separation with application in electrolytic production of gases in "zero-gap" cells.
Other embodiments of the invention are within the accompanying claims.
Claims (15)
1. A bipolar fluid flow field plate for a fuel cell comprising an
electrically conductive, non-porous sheet having a first fluid flow channel 5 patterned into a first face of the sheet and a second fluid flow channel patterned into the opposite face of the sheet, in which the pattern of the first channel is configured to have no portion thereof directly overlying the pattern of the second channel over a substantial area of the sheet.
10
2. The bipolar fluid flow field plate of claim 1 in which the pattern of
the first channel is configured to have no portion thereof directly overlying the pattern of the second channel over the entire area of the sheet.
3. The bipolar fluid flow field plate of claim 1 or claim 2 in which the
15 first fluid flow channel is formed in the first face of the sheet to a depth dA and the second fluid flow channel is formed in the opposite face of the sheet to a depth dc, the combined depths dA + dc being greater than the total plate thickness, Tp.
20
4. The bipolar fluid flow field plate of claim 3 in which the first fluid
flow channel and the second fluid flow channel are each formed to a depth that is greater than half the thickness of the plate.
5. The bipolar fluid flow field plate of claim 3 or claim 4 in which the
25 internal channel spacing between channels on opposing faces of the plate is at least 0.1 mm.
6. The bipolar fluid flow field plate of claim 1 having at least said first
fluid flow channels being discontinuous in the first face of the bipolar fluid 30 flow field plate, and further including a porous electrode mounted adjacent
to the first face, in which the porous electrode includes bypass channels co-
registered with the discontinuous flow channels in the bipolar fluid flow field plate so as to permit fluid communication between adjacent ends of
said discontinuous flow channels.
7. The bipolar fluid flow field plate of claim 6 in which the bypass
channels are arranged to overlie portions of the bipolar fluid flow field plate
where second fluid flow channels in the opposite face of the bipolar fluid flow field plate traverse the channel pattern in the first face.
8. A bipolar fluid flow field plate for a fuel cell comprising an
electrically conductive, non-porous sheet having a first fluid flow channel patterned into a first face of the sheet and a second fluid flow channel patterned into the opposite face of the sheet, in which the combined depth of 15 the first and second channels in an active area of the plate exceeds the total thickness of the plate.
9. The bipolar fluid flow field plate of claim 8 in which the depth of the
first channel and the depth of the second channel both each exceed half the 20 plate thickness.
10. The bipolar fluid flow field plate of claim 8 or claim 9 in which the
channel depths are substantially uniform across the entire active area of the plate.
11. The bipolar fluid flow field plate of any one of claims 8 to 10 having
at least said first fluid flow channel discontinuous in the first face of the bipolar fluid flow field plate, and further including a porous electrode
mounted adjacent to the first face, in which the porous electrode includes 30 bypass channels co-registered with the discontinuous flow channels in the
bipolar fluid flow field plate so as to permit fluid communication between
adjacent ends of said discontinuous flow channels.
12. The bipolar fluid flow field plate of claim 11 in which the bypass
5 channels are arranged to overlie portions of the bipolar fluid flow field plate
where second fluid flow channels in the opposite face of the bipolar fluid flow field plate traverse the channel pattern in the first face.
13. The bipolar fluid flow field plate of claim 1 or claim 8 having at least
10 said first fluid flow channels being discontinuous in the first face of the bipolar fluid flow field plate, and further including a porous electrode
mounted adjacent to the first face, in which the porous electrode permits fluid communication between adjacent ends of said discontinuous flow channels by forced diffusion through the porous electrode.
14. The bipolar fluid flow field plate of claim 13 in which the length of
the discontinuities in the first fluid flow channels lie in the range 0.1 mm to 2.0mm. 20
15. A fluid flow field plate substantially as described herein with
reference to the accompanying figures 5 to l Ob.
Priority Applications (11)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB0126688A GB2382455B (en) | 2001-11-07 | 2001-11-07 | Fuel cell fluid flow field plates |
CA2471122A CA2471122C (en) | 2001-11-07 | 2002-10-03 | Fuel cell fluid flow field plates |
EP02765083.7A EP1442491B1 (en) | 2001-11-07 | 2002-10-03 | Fuel cell fluid flow field plates |
BR0206313-1A BR0206313A (en) | 2001-11-07 | 2002-10-03 | Bipolar fluid flow field plate for a fuel cell |
JP2003543127A JP4700910B2 (en) | 2001-11-07 | 2002-10-03 | Fuel cell flow field plate |
MXPA04004279A MXPA04004279A (en) | 2001-11-07 | 2002-10-03 | Fuel cell fluid flow field plates. |
US10/494,628 US8304139B2 (en) | 2001-11-07 | 2002-10-03 | Fuel cell fluid flow field plates |
RU2004117094/09A RU2302689C2 (en) | 2001-11-07 | 2002-10-03 | Fuel-cell fluid medium flow distribution plates |
PCT/GB2002/004483 WO2003041199A2 (en) | 2001-11-07 | 2002-10-03 | Fuel cell fluid flow field plates |
ZA200304912A ZA200304912B (en) | 2001-11-07 | 2003-06-24 | Fuel cell fluid flow field plates. |
NO20033090A NO333667B1 (en) | 2001-11-07 | 2003-07-07 | Fuel cell flow plates |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB0126688A GB2382455B (en) | 2001-11-07 | 2001-11-07 | Fuel cell fluid flow field plates |
Publications (3)
Publication Number | Publication Date |
---|---|
GB0126688D0 GB0126688D0 (en) | 2002-01-02 |
GB2382455A true GB2382455A (en) | 2003-05-28 |
GB2382455B GB2382455B (en) | 2004-10-13 |
Family
ID=9925290
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB0126688A Expired - Lifetime GB2382455B (en) | 2001-11-07 | 2001-11-07 | Fuel cell fluid flow field plates |
Country Status (11)
Country | Link |
---|---|
US (1) | US8304139B2 (en) |
EP (1) | EP1442491B1 (en) |
JP (1) | JP4700910B2 (en) |
BR (1) | BR0206313A (en) |
CA (1) | CA2471122C (en) |
GB (1) | GB2382455B (en) |
MX (1) | MXPA04004279A (en) |
NO (1) | NO333667B1 (en) |
RU (1) | RU2302689C2 (en) |
WO (1) | WO2003041199A2 (en) |
ZA (1) | ZA200304912B (en) |
Cited By (1)
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---|---|---|---|---|
CN114824347A (en) * | 2022-03-31 | 2022-07-29 | 潍柴巴拉德氢能科技有限公司 | Bipolar plate and fuel cell |
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GB2412784B (en) * | 2002-01-18 | 2006-08-23 | Intelligent Energy Ltd | Fuel cell oxygen removal and pre-conditioning system |
GB2390738B (en) * | 2002-07-09 | 2005-05-11 | Intelligent Energy Ltd | Fuel cell direct water injection |
GB2401986B (en) * | 2003-05-17 | 2005-11-09 | Intelligent Energy Ltd | Improvements in fuel utilisation in electrochemical fuel cells |
GB2409763B (en) | 2003-12-31 | 2007-01-17 | Intelligent Energy Ltd | Water management in fuel cells |
GB2413002B (en) * | 2004-04-08 | 2006-12-06 | Intelligent Energy Ltd | Fuel cell gas distribution |
WO2005117177A1 (en) * | 2004-05-31 | 2005-12-08 | Toyota Jidosha Kabushiki Kaisha | Fuel cell |
KR100647666B1 (en) | 2004-11-29 | 2006-11-23 | 삼성에스디아이 주식회사 | Bipolar plate and direct liquid feed fuel cell stack |
GB2422716B (en) * | 2005-01-26 | 2007-08-22 | Intelligent Energy Ltd | Multi-layer fuel cell diffuser |
KR100627373B1 (en) * | 2005-04-08 | 2006-09-22 | 삼성에스디아이 주식회사 | Stack for fuel cell |
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CA2471122C (en) | 2010-11-30 |
NO333667B1 (en) | 2013-08-05 |
US20050048351A1 (en) | 2005-03-03 |
JP2005509260A (en) | 2005-04-07 |
GB0126688D0 (en) | 2002-01-02 |
WO2003041199A2 (en) | 2003-05-15 |
ZA200304912B (en) | 2004-09-27 |
NO20033090D0 (en) | 2003-07-07 |
BR0206313A (en) | 2004-02-10 |
CA2471122A1 (en) | 2003-05-15 |
US8304139B2 (en) | 2012-11-06 |
RU2302689C2 (en) | 2007-07-10 |
RU2004117094A (en) | 2005-11-20 |
GB2382455B (en) | 2004-10-13 |
EP1442491A2 (en) | 2004-08-04 |
MXPA04004279A (en) | 2005-05-16 |
WO2003041199A3 (en) | 2003-11-27 |
JP4700910B2 (en) | 2011-06-15 |
NO20033090L (en) | 2003-09-02 |
EP1442491B1 (en) | 2017-08-16 |
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PE20 | Patent expired after termination of 20 years |
Expiry date: 20211106 |